Fresenius Kabi Issues Critical Software Update for Ivenix Infusion Pumps
FDA identifies Class I recall as most serious type due to software anomalies that may cause unexpected shutdowns and interface freezing.
FDA identifies Class I recall as most serious type due to software anomalies that may cause unexpected shutdowns and interface freezing.
Fresenius Medical Care is recalling certain hemodialysis machines for a potential issue with patient exposure to hazardous chemicals.
Fresenius Kabi received a cybersecurity warning regarding its infusion pump system in which some components are susceptible to security vulnerabilities.
FDA identifies Class I recall as most serious type due to software anomalies that may cause unexpected shutdowns and interface freezing.